Linked Data
ClinVar Variation Id:
285872
dbSNP Id:
rs142169776
ExAC:
16:69368758 C / T
gnomAD v2:
16-69368758-C-T
gnomAD v3:
16-69334855-C-T
gnomAD v4:
16-69334855-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.69334855C>T , CM000678.2:g.69334855C>T | GRCh38 |
| NC_000016.9:g.69368758C>T , CM000678.1:g.69368758C>T | GRCh37 |
| NC_000016.8:g.67926259C>T | NCBI36 |
| NG_009013.1:g.9769G>A | |
| NG_033043.1:g.741G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306875.10:c.1079G>A MANE Select | ENSP00000305459.6:p.Gly360Glu | |
| ENST00000306875.8:c.1079G>A | ENSP00000305459.4:p.Gly360Glu | |
| ENST00000562081.2:c.1079G>A | ENSP00000455954.1:p.Gly360Glu | |
| ENST00000562595.5:c.549+471G>A | ||
| ENST00000562949.1:c.17G>A | ENSP00000457718.1:p.Gly6Glu | |
| NM_032382.4:c.1079G>A | NP_115758.3:p.Gly360Glu | |
| NM_001374871.1:c.1079G>A | NP_001361800.1:p.Gly360Glu | |
| NM_032382.5:c.1079G>A MANE Select | NP_115758.3:p.Gly360Glu | |
| NM_001379261.1:c.1079G>A | NP_001366190.1:p.Gly360Glu | |
| NM_001379262.1:c.1079G>A | NP_001366191.1:p.Gly360Glu | |
| NM_001379263.1:c.1079G>A | NP_001366192.1:p.Gly360Glu | |
| NM_001379264.1:c.1079G>A | NP_001366193.1:p.Gly360Glu | |
| NM_001379265.1:c.1079G>A | NP_001366194.1:p.Gly360Glu | |
| NM_001379266.1:c.1079G>A | NP_001366195.1:p.Gly360Glu |